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Featured researches published by Paul D. Hill.


Synthetic Communications | 2003

Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro- s-indacen-4-yl)-3-[4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Anti-inflammatory Agent

Frank J. Urban; V. John Jasys; Jeffrey W. Raggon; Richard A. Buzon; Paul D. Hill; James Frederick Eggler; John D. Weaver

Abstract A novel synthesis of the anti-inflammatory agent 1-(1,2,3,5,6,7- hexahydro-s-indacen-4-yl)-3-[4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl] urea 1 is described. Sulfonamide 5 was prepared starting from ethyl 3-furoate 2. Key steps were a one-pot sulfonylation with chlorosulfonic acid in methylene chloride followed by pyridinium salt formation and reaction with phosphorus pentachloride to provide ethyl 2-(chlorosulfonyl)-4-furoate 7. This sulfonyl chloride was treated with ammonium bicarbonate to form sulfonamide 8, followed by treatment with excess methyl magnesium chloride to provide 4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonamide 5. 4-Isocyanato-1,2,3,5,6,7-hexahydro-s-indacene 16 was prepared from indan in five steps. The formation of the desired sulfonyl urea was carried out both with the isolated isocyanate 16 and via an in situ method.


Synthesis | 1998

2,5-Dimethylpyrrole Protection Facilitates Copper(I)-Mediated Methoxylations of Aryl Iodides in the Presence of Anilines

John A. Ragan; Teresa W. Makowski; Michael J. Castaldi; Paul D. Hill


Synlett | 2004

Synthesis of N, N-dimethylpropanediamide and its utility for the preparation of 2-(acetamidomethyl)-4-aryloxazoles

John A. Ragan; Michael Burmaster; Paul D. Hill


Organic Syntheses | 2002

Ullman methoxylation in the presence of a 2,5-dimethylpyrrole-blocked aniline: Preparation of 2-fluoro-4-methoxyaniline (benzenamine, 2-fluoro-4-methoxy-)

John A. Ragan; Brian P. Jones; Michael J. Castaldi; Paul D. Hill; Teresa W. Makowski; Samuel W. Ridenour; David J. Hart


Organic Process Research & Development | 2012

A Scalable Synthesis of CE-157119 HCl Salt, an SRI/5-HT2A Antagonist

Yong Tao; Daniel W. Widlicka; Paul D. Hill; Michel Couturier; Gregory R. Young


Archive | 2000

Process for preparing cyclic thioamides

George J. Quallich; Jeffrey W. Raggon; Paul D. Hill


Archive | 1987

Processes for 2-(1-pentyl-3-guanidino)-4-(2-methyl-4-imidazolyl)thiazole and the crystalline dihydrochloride trihydrate thereof

Douglas John Meldrum Allen; William M Snyder; Berkeley W. Cue; Stanley Walter Walinsky; Paul D. Hill


Archive | 1986

Processes for 2-(1-pentyl-3-guanidino)-4-(2-methyl-4-imidazolyl) thiazole and analogs

Paul D. Hill; William M Snyder; Stanley William Walinsky


ChemInform | 2004

Synthetic, structural, and mechanistic issues in the development of a subtype selective GABA partial agonist hypnotic agent

John A. Ragan; Jerry Anthony Murry; Michael J. Castaldi; Alyson Kay Conrad; Paul D. Hill; Brian P. Jones; Narasimhan Kasthurikrishnan; Bryan Li; Teresa W. Makowski; Ruth E. McDermott; Barb J. Sitter; Timothy Donald White; Gregory R. Young


Organic Syntheses | 2003

Ullman Methoxylation in the Presence of a 2,5‐Dimethylpyrrole‐Blocked Aniline: Preparation of 2‐Fluoro‐4‐Methoxyaniline

John A. Ragan; Brian P. Jones; Michael J. Castaldi; Paul D. Hill; Teresa W. Makowski

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